DE2711235C2 - - Google Patents
Info
- Publication number
- DE2711235C2 DE2711235C2 DE2711235A DE2711235A DE2711235C2 DE 2711235 C2 DE2711235 C2 DE 2711235C2 DE 2711235 A DE2711235 A DE 2711235A DE 2711235 A DE2711235 A DE 2711235A DE 2711235 C2 DE2711235 C2 DE 2711235C2
- Authority
- DE
- Germany
- Prior art keywords
- reactor
- batch
- hydrocarbons
- hydrocarbon
- polymerized
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 229930195733 hydrocarbon Natural products 0.000 claims description 37
- 150000002430 hydrocarbons Chemical class 0.000 claims description 37
- 229920005989 resin Polymers 0.000 claims description 36
- 239000011347 resin Substances 0.000 claims description 36
- 239000003054 catalyst Substances 0.000 claims description 27
- 238000000034 method Methods 0.000 claims description 26
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 claims description 25
- 239000000203 mixture Substances 0.000 claims description 23
- 239000004215 Carbon black (E152) Substances 0.000 claims description 19
- 238000006116 polymerization reaction Methods 0.000 claims description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 16
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 claims description 15
- 238000004821 distillation Methods 0.000 claims description 15
- 229910015900 BF3 Inorganic materials 0.000 claims description 13
- 238000009835 boiling Methods 0.000 claims description 10
- 238000006243 chemical reaction Methods 0.000 claims description 9
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 8
- 239000007788 liquid Substances 0.000 claims description 8
- 239000012429 reaction media Substances 0.000 claims description 8
- 239000011541 reaction mixture Substances 0.000 claims description 8
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 claims description 7
- 238000000605 extraction Methods 0.000 claims description 7
- 239000000295 fuel oil Substances 0.000 claims description 7
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical class C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 claims description 6
- 238000004064 recycling Methods 0.000 claims description 6
- 239000013032 Hydrocarbon resin Substances 0.000 claims description 5
- 239000002841 Lewis acid Substances 0.000 claims description 5
- 229910021627 Tin(IV) chloride Inorganic materials 0.000 claims description 5
- 238000001914 filtration Methods 0.000 claims description 5
- 229920006270 hydrocarbon resin Polymers 0.000 claims description 5
- 150000007517 lewis acids Chemical class 0.000 claims description 5
- 239000000463 material Substances 0.000 claims description 5
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 claims description 5
- LRTOHSLOFCWHRF-UHFFFAOYSA-N 1-methyl-1h-indene Chemical compound C1=CC=C2C(C)C=CC2=C1 LRTOHSLOFCWHRF-UHFFFAOYSA-N 0.000 claims description 4
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 claims description 4
- 238000006386 neutralization reaction Methods 0.000 claims description 4
- QROGIFZRVHSFLM-UHFFFAOYSA-N prop-1-enylbenzene Chemical class CC=CC1=CC=CC=C1 QROGIFZRVHSFLM-UHFFFAOYSA-N 0.000 claims description 4
- 239000007864 aqueous solution Substances 0.000 claims description 3
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 3
- 238000010790 dilution Methods 0.000 claims description 3
- 239000012895 dilution Substances 0.000 claims description 3
- 238000001704 evaporation Methods 0.000 claims description 3
- 230000008020 evaporation Effects 0.000 claims description 3
- 239000011872 intimate mixture Substances 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 claims 5
- 239000000975 dye Substances 0.000 claims 2
- 239000012074 organic phase Substances 0.000 claims 2
- 238000010908 decantation Methods 0.000 claims 1
- 238000002955 isolation Methods 0.000 claims 1
- 230000000379 polymerizing effect Effects 0.000 claims 1
- 238000011144 upstream manufacturing Methods 0.000 claims 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 238000005406 washing Methods 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- ODLMAHJVESYWTB-UHFFFAOYSA-N propylbenzene Chemical compound CCCC1=CC=CC=C1 ODLMAHJVESYWTB-UHFFFAOYSA-N 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000008096 xylene Substances 0.000 description 3
- GWHJZXXIDMPWGX-UHFFFAOYSA-N 1,2,4-trimethylbenzene Chemical compound CC1=CC=C(C)C(C)=C1 GWHJZXXIDMPWGX-UHFFFAOYSA-N 0.000 description 2
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 238000010924 continuous production Methods 0.000 description 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 238000000197 pyrolysis Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 2
- KZMGYPLQYOPHEL-UHFFFAOYSA-N Boron trifluoride etherate Chemical compound FB(F)F.CCOCC KZMGYPLQYOPHEL-UHFFFAOYSA-N 0.000 description 1
- QROGIFZRVHSFLM-QHHAFSJGSA-N [(e)-prop-1-enyl]benzene Chemical compound C\C=C\C1=CC=CC=C1 QROGIFZRVHSFLM-QHHAFSJGSA-N 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000007970 homogeneous dispersion Substances 0.000 description 1
- AUHZEENZYGFFBQ-UHFFFAOYSA-N mesitylene Substances CC1=CC(C)=CC(C)=C1 AUHZEENZYGFFBQ-UHFFFAOYSA-N 0.000 description 1
- 125000001827 mesitylenyl group Chemical group [H]C1=C(C(*)=C(C([H])=C1C([H])([H])[H])C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229930015698 phenylpropene Natural products 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000004230 steam cracking Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F240/00—Copolymers of hydrocarbons and mineral oils, e.g. petroleum resins
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F12/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
- C08F12/02—Monomers containing only one unsaturated aliphatic radical
- C08F12/04—Monomers containing only one unsaturated aliphatic radical containing one ring
- C08F12/06—Hydrocarbons
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/584—Recycling of catalysts
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polymerisation Methods In General (AREA)
- Polymerization Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7607564A FR2344572A1 (fr) | 1976-03-16 | 1976-03-16 | Procede perfectionne de fabrication en continu de resines d'hydrocarbures |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2711235A1 DE2711235A1 (de) | 1978-02-02 |
| DE2711235C2 true DE2711235C2 (is") | 1988-09-29 |
Family
ID=9170505
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19772711235 Granted DE2711235A1 (de) | 1976-03-16 | 1977-03-15 | Verfahren zur kontinuierlichen herstellung von kohlenwasserstoffharzen |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US4100336A (is") |
| JP (1) | JPS5835528B2 (is") |
| BR (1) | BR7602711A (is") |
| DE (1) | DE2711235A1 (is") |
| FR (1) | FR2344572A1 (is") |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2506773B1 (fr) * | 1981-05-26 | 1986-02-21 | Charbonnages Ste Chimique | Resines d'hydrocarbures aromatiques contenant des groupes vinylcetone et leur application a l'obtention de polymeres par voie anionique |
| FR2510123A1 (fr) * | 1981-07-24 | 1983-01-28 | Charbonnages Ste Chimique | Polymeres de resines d'hydrocarbures aromatiques contenant des groupes vinylcetone et leur procede de preparation |
| JP3007118B2 (ja) * | 1990-06-29 | 2000-02-07 | ライオン株式会社 | 分散剤 |
| US5109081A (en) * | 1990-12-28 | 1992-04-28 | Exxon Chemical Patents, Inc. | Process for continuous thermal polymerization of cyclic hydrocarbon resins using recycle as a means of controlling molecular weight |
| US7517934B2 (en) * | 2003-07-31 | 2009-04-14 | Basf Corporation | Modified anionically polymerized polymers |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2340413A (en) * | 1941-07-12 | 1944-02-01 | Allied Chem & Dye Corp | Method for production of coumarone-indene type resins |
| US2565222A (en) * | 1948-06-30 | 1951-08-21 | Neville Co | Continuous process for the manufacture of monodispers coumaroneindene resins |
| US2697694A (en) * | 1950-10-28 | 1954-12-21 | Standard Oil Co | Manufacture of high molecular weight polybutenes |
| US2708639A (en) * | 1952-03-20 | 1955-05-17 | Du Pont | Polymers of butadiene-1, 3, process of making them, and compositions containing same |
| US2677002A (en) * | 1952-04-19 | 1954-04-27 | Standard Oil Co | Olefin polymerization with aluminum chloride-hydrocarbon complex catalyst |
| US2770613A (en) * | 1953-07-02 | 1956-11-13 | Exxon Research Engineering Co | Novel petroleum resin process |
| US3478005A (en) * | 1966-04-27 | 1969-11-11 | Neville Chemical Co | Terpene copolymers |
| GB1147019A (en) * | 1967-03-20 | 1969-04-02 | Solvay | Process and apparatus for polymerisation of olefins |
| JPS5033041B1 (is") * | 1970-07-22 | 1975-10-27 | ||
| DE2105561A1 (de) * | 1971-02-06 | 1972-08-17 | Ruetgerswerke Ag | Verfahren zur Herstellung von Inden Cumaron Harzen durch kationische Polymerisation von Ungesättigte enthal tenden Kohlenwasserstoff Fraktionen |
| US3799913A (en) | 1971-12-30 | 1974-03-26 | Neville Chemical Co | Production of hydrocarbon resin compositions from alpha-methyl styrene,indene and vinyl toluene |
| US3846352A (en) * | 1972-01-20 | 1974-11-05 | Goodyear Tire & Rubber | Pressure sensitive adhesive compositions comprising rubber and a resinous interpolymer |
| ES425173A1 (es) | 1973-07-14 | 1976-06-16 | Rutgerswerke Akiengesellschaft | Procedimiento para la preparacion de indeno. |
-
1976
- 1976-03-16 FR FR7607564A patent/FR2344572A1/fr active Granted
- 1976-04-30 BR BR7602711A patent/BR7602711A/pt unknown
-
1977
- 1977-03-15 JP JP52029120A patent/JPS5835528B2/ja not_active Expired
- 1977-03-15 DE DE19772711235 patent/DE2711235A1/de active Granted
- 1977-03-16 US US05/778,300 patent/US4100336A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| BR7602711A (pt) | 1977-11-01 |
| DE2711235A1 (de) | 1978-02-02 |
| FR2344572B1 (is") | 1979-04-06 |
| JPS5835528B2 (ja) | 1983-08-03 |
| JPS52111991A (en) | 1977-09-20 |
| FR2344572A1 (fr) | 1977-10-14 |
| US4100336A (en) | 1978-07-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2531210A1 (de) | Gemisch auf basis eines paraffinischen grundoels | |
| DE715045C (de) | Verfahren zur Herstellung von in aliphatischen Kohlenwasserstoffen loeslichen Harzen | |
| DE855292C (de) | Synthetische trocknende OEle bzw. Lackgrundstoffe oder Lacke und Verfahren zu deren Herstellung | |
| DE2711235C2 (is") | ||
| DE2144255B2 (de) | Verfahren zur Herstellung von Erdölharzen | |
| DE2029416A1 (de) | Verfahren zur Herstellung von flus sigen Pols nieren | |
| DE2259972A1 (de) | Petroleumharze | |
| DE1103588B (de) | Verfahren zur Herstellung von Mischpolymerisaten des p- oder m-Diisopropenylbenzols | |
| DE2364169A1 (de) | Verfahren zur herstellung von petroleumharzen | |
| DE1443007A1 (de) | Polymere von aromatischen Verbindungen und Verfahren zu deren Herstellung | |
| DE69433162T2 (de) | Harzartiges copolymer enthaltend einheiten von phenolverbindungen und von olefinisch ungesättigten nichtsauren terpenverbindungen. | |
| DE2163525A1 (de) | Verfahren zur Herstellung von in organischen Lösungsmitteln löslichen Harzen mit auf einen vorbestimmten Wert einstellbarem Erweichungspunkt | |
| DE1470573A1 (de) | Verfahren zur Reinigung von Koksofen-Leichtoel | |
| DE912021C (de) | Verfahren zum fortlaufenden Mischpolymerisieren eines niedrigen aliphatischen Monoolefins mit einem polymerisierbaren, einen aromatischen Kern enthaltenden Monoolefin | |
| DE2943147C2 (is") | ||
| DE2429295A1 (de) | Verfahren zur herstellung von petrolharzen | |
| DE1109900B (de) | Verfahren zur Herstellung trocknender polymerer Kohlenwasserstoffoele | |
| DE1062854B (de) | Verfahren zur Stabilisierung der Viskositaet der Loesungen oxydierter, synthetischer trocknender OEle | |
| EP0070579B1 (de) | Kohlenwasserstoffharze mit einer OH-Zahl grösser als 6 und mit schwachem Phenolgeruch sowie Verfahren zu ihrer Herstellung | |
| DE2754047A1 (de) | Verfahren zur herstellung eines niedermolekularen polymers | |
| DE1053784B (de) | Verfahren zur Erhoehung des Erweichungspunktes von Erdoel-Kohlenwasserstoff-Harzen | |
| DE1118459B (de) | Verfahren zur Herstellung von Mischpolymerisaten | |
| DE1037134B (de) | Verfahren zur Herstellung eines synthetischen trocknenden OEles durch Polymerisationbzw. Mischpolymerisation | |
| DE1213614B (de) | Verfahren zur Herstellung eines Pfropfpolymerisats | |
| DE1620794A1 (de) | Erdoelharz-Wachsmasse und Verfahren zur Herstellung derselben |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8110 | Request for examination paragraph 44 | ||
| D2 | Grant after examination | ||
| 8363 | Opposition against the patent | ||
| 8327 | Change in the person/name/address of the patent owner |
Owner name: NORSOLOR S.A., COURBEVOIE, FR |
|
| 8328 | Change in the person/name/address of the agent |
Free format text: HAFT, U., DIPL.-PHYS., 8000 MUENCHEN BERNGRUBER, O., DIPL.-CHEM. DR.RER.NAT., 8232 BAYERISCH GMAIN CZYBULKA, U., DIPL.-PHYS., PAT.-ANWAELTE, 8000 MUENCHEN |
|
| 8331 | Complete revocation |